机构:
Duke Univ, Duke Mol Physiol Inst, Durham, NC 27701 USADuke Univ, Duke Mol Physiol Inst, Durham, NC 27701 USA
Gray, Sarah M.
[1
]
Page, Laura C.
论文数: 0引用数: 0
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机构:
Duke Univ, Dept Pediat, Div Endocrinol, Durham, NC 27706 USADuke Univ, Duke Mol Physiol Inst, Durham, NC 27701 USA
Page, Laura C.
[2
]
Tong, Jenny
论文数: 0引用数: 0
h-index: 0
机构:
Duke Univ, Duke Mol Physiol Inst, Durham, NC 27701 USA
Duke Univ, Dept Med, Div Endocrinol Metab & Nutr, Durham, NC USADuke Univ, Duke Mol Physiol Inst, Durham, NC 27701 USA
Tong, Jenny
[1
,3
]
机构:
[1] Duke Univ, Duke Mol Physiol Inst, Durham, NC 27701 USA
[2] Duke Univ, Dept Pediat, Div Endocrinol, Durham, NC 27706 USA
[3] Duke Univ, Dept Med, Div Endocrinol Metab & Nutr, Durham, NC USA
Ghrelin and its receptor, the growth hormone secretagogue receptor 1a (GHSR1a), are implicated in the regulation of glucose metabolism via direct actions in the pancreatic islet, as well as peripheral insulin-sensitive tissues and the brain. Although many studies have explored the role of ghrelin in glucose tolerance and insulin secretion, a complete mechanistic understanding remains to be clarified. This review highlights the local expression and function of ghrelin and GHSR1a in pancreatic islets and how this axis may modulate insulin secretion from pancreatic beta-cells. Additionally, we discuss the effect of ghrelin on in vivo glucose metabolism in rodents and humans, as well as the metabolic circumstances under which the action of ghrelin may predominate.
机构:
Department of Cell Metabolism and Nutrition, Brain/Liver Interface Medicine Research Center, Kanazawa University, Kanazawa, 920-8640, IshikawaDepartment of Cell Metabolism and Nutrition, Brain/Liver Interface Medicine Research Center, Kanazawa University, Kanazawa, 920-8640, Ishikawa